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Evolution and transition of expression trajectory during human brain development

机译:人脑发展中表达轨迹的演变与转变

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The remarkable abilities of the human brain are distinctive features that set us apart from other animals. However, our understanding of how the brain has changed in the human lineage remains incomplete, but is essential for understanding cognition, behavior, and brain disorders in humans. Here, we compared the expression trajectory in brain development between humans and rhesus macaques (Macaca mulatta) to explore their divergent transcriptome profiles. Results showed that brain development could be divided into two stages, with a demarcation date in a range between 25 and 26 postconception weeks (PCW) for humans and 17-23PCWfor rhesus macaques, rather than birth time that have been widely used as a uniform demarcation time of neurodevelopment across species. Dynamic network biomarker (DNB) analysis revealed that the two demarcation dates were transition phases during brain development, after which the brain transcriptome profiles underwent critical transitions characterized by highly fluctuating DNB molecules. We also found that changes between early and later brain developmental stages (as defined by the demarcation points) were substantially greater in the human brain than in the macaque brain. To explore the molecular mechanism underlying prolonged timing during early human brain development, we carried out expression heterochrony tests. Results demonstrated that compared to macaques, more heterochronic genes exhibited neoteny during early human brain development, consistent with the delayed demarcation time in the human lineage, and proving that neoteny in human brain development could be traced to the prenatal period. We further constructed transcriptional networks to explore the profile of early human brain development and identified the hub gene RBFOX1 as playing an important role in regulating early brain development. We also found RBFOX1 evolved rapidly in its non-coding regions, indicating that this gene played an important role in human brain evolution. Our findings provide evidence that RBFOX1 is a likely key hub gene in early human brain development and evolution. By comparing gene expression profiles between humans and macaques, we found divergent expression trajectories between the two species, which deepens our understanding of the evolution of the human brain.
机译:人类大脑的显着能力是与其他动物分开的独特功能。然而,我们对大脑在人体谱系中改变的了解仍然不完整,但对于了解人类的认知,行为和脑疾病至关重要。在这里,我们将人类和恒河猴(Macaca Mulatta)之间的脑部发展中的表达轨迹进行了比较探索其发散的转录组谱。结果表明,大脑发育可分为两个阶段,分界日期为25至26周(PCW)的范围,为人类和17-23pcwfor恒河猴,而不是被广泛用作统一划分的出生时间在物种中神经发育的时间。动态网络生物标志物(DNB)分析显示,两种分界日期是脑发育过程中的转型相,之后脑转录组谱接受了由高波动的DNB分子特征的关键转变。我们还发现,人类大脑的早期和后期脑发育阶段(如划分点所定义)的变化比在猕猴脑中大致更大。为了探讨早期人脑发育期间延长时间延长的分子机制,我们进行了表达异形检查。结果表明,与猕猴相比,更多的异形基因在早期的人脑发育过程中表现出奈良,与人类血统中的延迟分界时间一致,并证明人脑发育中的雷弱可以追溯到产前期。我们进一步建立了转录网络,探讨了早期人脑发育的概况,并确定了集线器基因RBFOX1,因为在调节早期大脑发育方面发挥着重要作用。我们还发现RBFOX1在其非编码区域中快速发展,表明该基因在人脑进化中发挥着重要作用。我们的调查结果提供了RBFOX1是早期人脑发育和演变的一个可能的关键中心基因。通过比较人类和猕猴之间的基因表达谱,我们发现两种物种之间的发散表达轨迹,这会加深我们对人脑演变的理解。

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